Results 21 to 30 of about 212 (130)

Sertoli–Leydig cell tumors of ovary

Medicine, 2018
Abstract Introduction: The purpose of this study was to report the clinical features, computed tomography (CT) and magnetic resonance imaging (MRI) findings, clinical management, and prognoses of 7 patients with Sertoli–Leydig cell tumors (SLCT) of ovary, and to review the literature of this rare condition.
Xu, Qiong, Zou, Yu, Zhang, Xiao Fei
openaire   +2 more sources

A Sertoli-Leydig ovarian tumor presenting as ovarian torsion: A case report

Case Reports in Women's Health
Torsion occurs as a complication in 10% of cases of ovarian tumors. It predominantly occurs in benign ones, while malignant tumors are less prone to torsion.
Samia Tligui, Hounaida Mahfoud, Samia Sassi, Hanane Inrhaoun, Najat Lamalmi, Fatima El Hassouni, Samir Bargach   +6 more
doaj   +1 more source

Virilization in a postmenopausal female due to androgen secreting ovarian dermoid cyst

Journal of Mid-Life Health, 2017
Virilizing ovarian dermoid cysts are very rare. The source of androgen in these cysts may be tumors such as Sertoli–Leydig cell tumor or Leydig cell hyperplasia.
Murali Subbaiah, Gowri Dorairajan, Debasis Gochhait, G Vijayalakshmi   +3 more
doaj   +1 more source

Cytoreduction with hyperthermic intra peritoneal and intra thoracic chemotherapy for metastatic Sertoli-Leydig cell tumor of the ovary

Gynecologic Oncology Reports, 2020
Sertoli Leydig cell tumor (SLCT) is a rare sex-cord stromal tumor of the ovary that generally has a benign course. Here, we report an unusual case of recurrent, metastatic SLCT and its unique management with a combination of cytoreductive surgery ...
Nicholas K. Larsen, Matthew J. Reilly, Seunghyug Kwon, Brian W. Loggie, Marcus W. Balters   +4 more
doaj   +1 more source

Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor in a 16-Year-Old Single Woman: A Case Report and Literature Review

Case Reports in Obstetrics and Gynecology, 2013
Sertoli-Leydig cell tumor (SLCT) of ovary is an exceedingly unusual neoplasm that belongs to a group of sex cord-stromal tumors of ovary and accounts for less than 0.5% of all primary ovarian neoplasms.
Ahmed Abu-Zaid, Ayman Azzam, Lama Abdulhamid Alghuneim, Mona Tarek Metawee, Tarek Amin, Turki Omar Al-Hussain   +5 more
doaj   +1 more source

Leydig Cell Tumor in Children: a Case Report and Literature Review

Translational Research in Urology, 2020
Introduction Leydig cell tumors (LCTs) comprising of 1 to 3 percent of testicular cancers in children, one of the single most common symptoms in prepubertal patients is painless testicular swelling with or without a sign of precocious puberty.
Khashayar Atqiaee, Arash Mohammadi Tofigh, Shahab Salehpour, Alireza Mirshemirani   +3 more
doaj   +1 more source

15-Year-Old Patient with an Unusual Alpha-Fetoprotein-Producing Sertoli-Leydig Cell Tumor of Ovary

Case Reports in Obstetrics and Gynecology, 2022
Ovarian Sertoli-Leydig cell tumors (SLCTs) are extremely rare ovarian sex-cord stromal tumors. Alpha-fetoprotein (AFP) production by SLCTs is a rare event generally linked to the presence of hepatocytes or intestinal mucinous epithelium as heterologous ...
Kaçar Serife, Stavros Karampelas, Nathalie Hottat, Christine Devalck, Katherina Vanden Houte   +4 more
doaj   +1 more source

SERTOLI-LEYDIG CELL TUMOR; A RARE CASE IN A POSTMENOPAUSAL PATIENT – CASE REPORT

Zdravniški Vestnik, 2018
Background. Sertoli-Leydig cell tumors belong to the group of sex cord stromal tumors of the ovary. They account for less than 0.5 % of all ovarian tumors and occur primarily in young women between 20 and 30 years of age.
Petra Krajnc, Borut Gorišek, Dejan Ognjenovik, Damijana Bosilj   +3 more
doaj   +1 more source

Evaluation of therapeutic effects of D‐limonene following orchiopexy in the rat model of cryptorchidism

Animal Models and Experimental Medicine, EarlyView.
D‐limonene supplementation enhances testicular recovery following orchiopexy in a rat model of bilateral cryptorchidism. Treatment with D‐limonene reduces oxidative stress (↓MDA, ↑SOD, ↑GPx, ↑TAC), downregulates pro‐apoptotic proteins (↓TNF‐α, ↓BAX, ↓Caspase‐3), and upregulates anti‐apoptotic Bcl‐2 expression.
Arman Norouzi‐Ghalehbala, Mohammadjavad Rezaei‐Varmaziar, Majid Taati, Ali Soleimanzadeh, Abbas Raisi, Farshid Davoodi, Amir Ali Shahbazfar   +6 more
wiley   +1 more source

Case report of a 3-year-old girl with pleuropulmonary blastoma and family history of a tumor predisposition syndrome with c. 2830 gene mutation in DICER1

Journal of Pediatric Surgery Case Reports, 2015
Pleuropulmonary blastoma (PPB) is a childhood mesenchymal pleural-based tumor that is associated with a germline mutation in DICER1 gene in familial PPB. It occurs most commonly in children between the ages of 2 and 5.
Y. Puckett, J. Howe, D. Vane, A. Agarwal, J.R. Batanian, J. Greenspon   +5 more
doaj   +1 more source